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Laser Sun Block 100 SPF50 - 76344-4001-2 - (OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE)

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Drug Information of Laser Sun Block 100 SPF50

Product NDC: 76344-4001
Proprietary Name: Laser Sun Block 100 SPF50
Non Proprietary Name: OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Active Ingredient(s): 7.5; 5; 2.49; 4.8    g/100mL; g/100mL; g/100mL; g/100mL & nbsp;   OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Laser Sun Block 100 SPF50

Product NDC: 76344-4001
Labeler Name: Humex,Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130515

Package Information of Laser Sun Block 100 SPF50

Package NDC: 76344-4001-2
Package Description: 1 TUBE in 1 BOX (76344-4001-2) > 50 mL in 1 TUBE (76344-4001-1)

NDC Information of Laser Sun Block 100 SPF50

NDC Code 76344-4001-2
Proprietary Name Laser Sun Block 100 SPF50
Package Description 1 TUBE in 1 BOX (76344-4001-2) > 50 mL in 1 TUBE (76344-4001-1)
Product NDC 76344-4001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130515
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Humex,Inc.
Substance Name OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 7.5; 5; 2.49; 4.8
Strength Unit g/100mL; g/100mL; g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of Laser Sun Block 100 SPF50


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